about
FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardationHuman osteoarthritic chondrocytes exposed to extremely low-frequency electromagnetic fields (ELF) and therapeutic application of musically modulated electromagnetic fields (TAMMEF) systems: a comparative study.Histopathological findings in systemic sclerosis-related myopathy: fibrosis and microangiopathy with lack of cellular inflammation.D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings.Alternative Pathways of Cancer Cell Death by Rottlerin: Apoptosis versus Autophagy.Paraneoplastic necrotizing myopathy associated with adenocarcinoma of the lung - a rare entity with atypical onset: a case report.Geometric complexity identifies platelet activation in familial hypercholesterolemic patients.Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy.Endothelin-1 and endothelin-converting enzyme-1 in human granulomatous pathology of eyelid: an immunohistochemical and in situ hybridization study in chalazia.Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.Sensory-motor axonal multineuropathy during etanercept therapy for rheumatoid arthritis.The role of preoperative oxidative stress and mandibular third molar postoperative outcome.F2-Isoprostanes in soft oral tissues and degree of oral disability after mandibular third molar surgery.Calf muscle hypertrophy following S1 radiculopathy: A stress disorder caused by hyperactivity with variable response to treatmen.Peptidergic innervation of mesenteric lymphatics in guinea pigs: an immunocytochemical and pharmacological study.Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal.A case of amyloid myopathy in a patient with familial Mediterranean feverEosinophilia-associated muscle disorders: an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological formsUncommon findings in idiopathic hypertrophic cranial pachymeningitisMuscle mitochondrial changes in cerebrotendinous xanthomatosisVitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case reportFamilial multiple exostoses syndrome: a phacomatosis of bone tissueLymphatic vessels in human sural nerve: immunohistochemical detection by D2-40Lymphatic vessels in human eyelids: an immunohistological study in dermatochalasis and chalazionTwo families with novel PMP22 point mutations: genotype-phenotype correlationExpression of RXFP1 in skin of scleroderma patients and control subjectsIs osteopontin involved in cutaneous fibroblast activation? Its hypothetical role in scleroderma pathogenesis
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nila Volpi
@ast
Nila Volpi
@en
Nila Volpi
@es
Nila Volpi
@nl
type
label
Nila Volpi
@ast
Nila Volpi
@en
Nila Volpi
@es
Nila Volpi
@nl
prefLabel
Nila Volpi
@ast
Nila Volpi
@en
Nila Volpi
@es
Nila Volpi
@nl
P106
P31
P496
0000-0002-0837-1864